Determine the necessary mass, volume, or concentration for preparing a solution.
Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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SKU | Size | Availability | Price | Qty |
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M275233-5mg | 5mg | In stock | $151.90 | |
M275233-10mg | 10mg | In stock | $205.90 | |
M275233-25mg | 25mg | In stock | $423.90 | |
M275233-50mg | 50mg | In stock | $763.90 |
Selective A 2B antagonist
Synonyms | N-(4-cyanophenyl)-2-[4-(2,6-dioxo-1,3-dipropyl-7H-purin-8-yl)phenoxy]acetamide | (4-Cyano-phenyl)-carbamic acid 4-(2,6-dioxo-1,3-dipropyl-2,3,6,7-tetrahydro-1H-purin-8-yl)-phenyl ester | AKOS000346342 | HY-14121 | Lopac0_000729 | 7E435V2DAH | AI3-10031 | |
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Specifications & Purity | Moligand™, ≥98% |
Biochemical and Physiological Mechanisms | Selective A 2B antagonist (K i values are 1.97 (hA 2B ), 403 (hA 1 ), 503 (hA 2A ), and 570 nM (hA 3 ).MRS 1754 is a p-cyanoanilide xanthine derivative. It might act as a potential anti-asthmatic drug. MRS 1754 is a potent A2B adenosine receptor antagonis |
Storage Temp | Store at -20°C,Desiccated |
Shipped In | Ice chest + Ice pads |
Grade | Moligand™ |
Action Type | ANTAGONIST |
Mechanism of action | Antagonist of A 1 receptor;Antagonist of A 2A receptor;Antagonist of A 2B receptor;Antagonist of A 3 receptor |
Note | Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details. |
Product Description | MRS 1754 is a selective antagonist radioligand for A2B adenosine receptor with very low affinity for A1 and A3 receptors of both humans and rats。 |
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IUPAC Name | N-(4-cyanophenyl)-2-[4-(2,6-dioxo-1,3-dipropyl-7H-purin-8-yl)phenoxy]acetamide |
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INCHI | InChI=1S/C26H26N6O4/c1-3-13-31-24-22(25(34)32(14-4-2)26(31)35)29-23(30-24)18-7-11-20(12-8-18)36-16-21(33)28-19-9-5-17(15-27)6-10-19/h5-12H,3-4,13-14,16H2,1-2H3,(H,28,33)(H,29,30) |
InChi Key | AJBBEYXFRYFVNM-UHFFFAOYSA-N |
Canonical SMILES | CCCN1C2=C(C(=O)N(C1=O)CCC)NC(=N2)C3=CC=C(C=C3)OCC(=O)NC4=CC=C(C=C4)C#N |
Isomeric SMILES | CCCN1C2=C(C(=O)N(C1=O)CCC)NC(=N2)C3=CC=C(C=C3)OCC(=O)NC4=CC=C(C=C4)C#N |
Alternate CAS | 264622-58-4 |
PubChem CID | 6603931 |
MeSH Entry Terms | 8-(4-(((4-cyanophenyl)carbamoylmethyl)oxy)phenyl)-1,3-di(ni-propyl)xanthine;MRS 1754;MRS-1754;MRS1754;N-(4-cyanophenyl)-2-(4-(2,3,6,7-tetrahydro-2,6-dioxo-1,3-dipropyl-1H-purin-8-yl)-phenoxy)acetamide |
Molecular Weight | 486.52 |
Enter Lot Number to search for COA:
Find and download the COA for your product by matching the lot number on the packaging.
Lot Number | Certificate Type | Date | Item |
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B2320383 | Certificate of Analysis | Dec 18, 2023 | M275233 |
B2320426 | Certificate of Analysis | Dec 18, 2023 | M275233 |
B2320431 | Certificate of Analysis | Dec 18, 2023 | M275233 |
B2320511 | Certificate of Analysis | Dec 18, 2023 | M275233 |
Solubility | Soluble in DMSO to 50 mM |
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Pictogram(s) | GHS07 |
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Signal | Warning |
Hazard Statements | H302:Harmful if swallowed |
Precautionary Statements | P501:Dispose of contents/container to ... P264:Wash hands [and …] thoroughly after handling. P270:Do not eat, drink or smoke when using this product. P330:Rinse mouth. P301+P317:IF SWALLOWED: Get medical help. |
1. Yi X et al.. (2018) Adenosine receptors enhance the ATP-induced odontoblastic differentiation of human dental pulp cells.. Biochem Biophys Res Commun, 497 (3): (850-856). [PMID:29454963] |
2. Basu M et al.. (2020) Increased host ATP efflux and its conversion to extracellular adenosine is crucial for establishing Leishmania infection.. J Cell Sci, 133 (7): [PMID:32079656] |
3. Zhou Y et al.. (2019) MRS1754 inhibits proliferation and migration of bladder urothelial carcinoma by regulating mitogen-activated protein kinase pathway.. J Cell Physiol, 234 (7): (11360-11368). [PMID:30565699] |